Quality Manager

Our client is a global medical device manufacturer.

• Bachelor’s degree in Engineering, Quality, or related field.
• 5–7+ years of experience in quality management within medical device, pharma, or other regulated manufacturing environments.
• Strong knowledge of FDA QSR, ISO 13485, and regulatory compliance.
• Solid experience in QMS, auditing, CAPA, and process improvement.
• Proven leadership and change management capability.
• Good business and operational mindset.
• Excellent communication skills; fluent in English.

If you are keen on the role, please directly contact Ms. Khanh Vy for immediate support via email: khanhvy.nguyen@adecco.com or zalo: 0908609952

• Lead overall quality activities of the plant to ensure product safety, compliance, and stable manufacturing performance.
• Build, maintain, and continuously improve the Quality Management System in line with FDA, ISO 13485, and other applicable regulations.
• Manage internal & external audits, inspections, and follow-up actions to closure.
• Drive CAPA, risk management, and continuous improvement initiatives across operations.
• Act as Management Representative for the QMS and main contact with regulatory bodies and auditors.
• Partner with production, engineering, supply chain, and suppliers to ensure quality standards are met throughout the value chain.
• Develop and coach the quality team to strengthen capability and ownership.